annotate mapper.xml @ 0:af18bb0baa92 draft

Imported from capsule None
author rnateam
date Tue, 27 Jan 2015 09:06:06 -0500
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children 12fc62b7dc09
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1 <tool id="rbc_mirdeep2_mapper" name="MiRDeep2 Mapper" version="2.0.0">
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2 <macros>
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3 <macro name="map_params">
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4 <conditional name="refGenomeSource">
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5 <param name="genomeSource" type="select" label="Will you select a reference genome from your history or use a built-in index?" help="Map to genome. (-p)">
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6 <option value="indexed">Use a built-in index</option>
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7 <option value="history">Use one from the history</option>
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8 </param>
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9 <when value="indexed">
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10 <param name="index" type="select" label="Select a reference genome" help="If your genome of interest is not listed, contact your Galaxy admin.">
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11 <options from_data_table="bowtie_indexes">
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12 <filter type="sort_by" column="2"/>
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13 <validator type="no_options" message="No indexes are available for the selected input dataset"/>
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14 </options>
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15 </param>
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16 </when> <!-- build-in -->
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17 <when value="history">
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18 <param name="ownFile" type="data" format="fasta" metadata_name="dbkey" label="Select the reference genome" />
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19 </when> <!-- history -->
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20 </conditional> <!-- refGenomeSource -->
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21 <param name="map_mismatch" type="boolean" truevalue="-q" falsevalue="" checked="false" label="Map with one mismatch in the seed (mapping takes longer)" help="(-q)"/>
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22 <param name="map_threshold" value="5" type="integer" optional="false" label="A read is allowed to map up to this number of positions in the genome" help="Map threshold. (-r)">
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23 <validator type="in_range" min="1" message="Minimum value is 1"/>
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24 </param>
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25 </macro>
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26 </macros>
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27 <description>
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28 <![CDATA[
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29 process and map reads to a reference genome
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30 ]]>
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31 </description>
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32 <requirements>
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33 <requirement type="package" version="2.0">mirdeep2_mapper</requirement>
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34 <requirement type="package" version="0.12.7">bowtie</requirement>
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35 <requirement type="package" version="5.18.1">perl</requirement>
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36 </requirements>
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37
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38 <command>
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39 <![CDATA[
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40
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41 #if $operation.collapse_map == "collapse_and_map" or $operation.collapse_map == "only_map"
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42 #if $operation.refGenomeSource.genomeSource == "history"
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43 bowtie-build $operation.refGenomeSource.ownFile custom_bowtie_indices &&
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44 #end if
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45 #end if
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46 mapper.pl
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47
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48 $reads
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49
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50 #if $reads.extension.startswith("fasta")
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51 -c
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52 #else if $reads.extension.startswith("fastq")
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53 -e -h
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54 #end if
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55
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56 $remove_non_canon
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57
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58 $convert_rna_dna
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59
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60 #if $clip_adapter.clip == "true"
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61 -k $clip_adapter.adapter_seq
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62 #end if
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63
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64 -l $discard_short_reads
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65
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66 #if $operation.collapse_map == "collapse_and_map" or $operation.collapse_map == "only_collapse"
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67 -m -s $output_reads_collapsed
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68 #end if
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69
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70 #if $operation.collapse_map == "collapse_and_map" or $operation.collapse_map == "only_map"
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71 -p
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72
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73 #if $operation.refGenomeSource.genomeSource == "history"
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74 custom_bowtie_indices
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75 #else
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76 $index
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77 #end if
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78
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79 $operation.map_mismatch
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80
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81 -r $operation.map_threshold
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82
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83 -t $output_mapping
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84 #end if
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85
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86 -v -n
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87 ]]>
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88 </command>
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89 <stdio>
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90 <!-- Anything other than zero is an error -->
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91 <exit_code range="1:" />
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92 <exit_code range=":-1" />
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93 <!-- In case the return code has not been set propery check stderr too -->
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94 <regex match="Error:" />
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95 <regex match="Exception:" />
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96 </stdio>
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97 <inputs>
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98 <param format="fastq, fasta" name="reads" type="data" optional="false" label="Deep sequencing reads" help="Reads in fastq or fasta format"/>
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99 <param name="remove_non_canon" type="boolean" truevalue="-j" falsevalue="" checked="false" label="Remove reads with non-standard nucleotides" help="Remove all entries that have a sequence that contains letters other than a,c,g,t,u,n,A,C,G,T,U,N. (-j)"/>
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100 <param name="convert_rna_dna" type="boolean" truevalue="-i" falsevalue="" checked="false" label="Convert RNA to DNA alphabet (to map against genome)" help="(-i)"/>
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101
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102 <conditional name="clip_adapter">
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103 <param name="clip" type="select" label="Clip 3' Adapter Sequence" help="(-k)">
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104 <option value="false">Don't Clip</option>
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105 <option value="true">Clip Sequence</option>
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106 </param>
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107 <when value="true">
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108 <param name="adapter_seq" value="" type="text" optional="false" label="Sequence to clip" help="Adapter Sequence can only contain a,c,g,t,u,n,A,C,G,T,U,N">
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109 <validator type="regex" message="Adapter can ONLY contain a,c,g,t,u,n,A,C,G,T,U,N">^[ACGTUacgtu]+$</validator>
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110 </param>
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111 </when>
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112 <when value="false"/>
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113 </conditional>
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114
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115 <param name="discard_short_reads" value="18" type="integer" optional="false" label="Discard reads shorter than this length" help="Set to 0 to keep all reads. (-l)">
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116 <validator type="in_range" min="0" message="Minimum value is 0"/>
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117 </param>
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118
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119 <conditional name="operation">
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120 <param name="collapse_map" type="select" label="Collapse reads and/or Map" help="(-m) and/or (-p)">
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121 <option value="collapse_and_map">Collapse reads and Map</option>
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122 <option value="only_map">Map</option>
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123 <option value="only_collapse">Collapse</option>
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124 </param>
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125 <when value="collapse_and_map">
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126 <expand macro="map_params"/>
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127 </when>
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128 <when value="only_map">
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129 <expand macro="map_params"/>
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130 </when>
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131 <when value="only_collapse"/>
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132 </conditional>
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133 </inputs>
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134 <outputs>
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135 <data format="fasta" name="output_reads_collapsed" label="Collapsed reads of ${tool.name} on ${on_string}">
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136 <filter>
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137 (
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138 operation['collapse_map'] == "collapse_and_map" or
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139 operation['collapse_map'] == "only_collapse"
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140 )
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141 </filter>
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142 </data>
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143 <data format="tabular" name="output_mapping" label="Mapping output of ${tool.name} on ${on_string} in ARF format">
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144 <filter>
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145 (
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146 operation['collapse_map'] == "collapse_and_map" or
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147 operation['collapse_map'] == "only_map"
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148 )
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149 </filter>
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150 </data>
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151 </outputs>
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152 <tests>
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153 <test>
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154 <param name="reads" value="reads.fa"/>
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155 <param name="remove_non_canon" value="True"/>
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156 <param name="clip" value="true"/>
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157 <param name="adapter_seq" value="TCGTATGCCGTCTTCTGCTTGT"/>
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158 <param name="discard_short_reads" value="18"/>
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159 <param name="collapse_map" value="collapse_and_map"/>
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160 <param name="genomeSource" value="history"/>
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161 <param name="ownFile" value="cel_cluster.fa"/>
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162 <output name="output_reads_collapsed">
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163 <assert_contents>
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164 <has_text text=">seq_349713_x268"/>
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165 <has_text text="TCACCGGGTGTANATCAGCTAA"/>
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166 <has_text text=">seq_354255_x214"/>
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167 <has_text text="TAACCGGGTGAACACTTGCAGT"/>
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168 <has_text text=">seq_357284_x187"/>
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169 </assert_contents>
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170 </output>
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171 <output name="output_mapping">
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172 <assert_contents>
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173 <has_line_matching expression="^.*22\t1\t22\ttcaccgggtggaaactagcagt\tchrII:11534525-11540624\t22\t3060\t3081.*$"/>
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174 <has_line_matching expression="^.*22\t1\t22\ttcaccgggtggaaactagtagt\tchrII:11534525-11540624\t22\t3060\t3081.*$"/>
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175 <has_line_matching expression="^.*22\t1\t22\ttcaccgggtgtacatcagcgaa\tchrII:11534525-11540624\t22\t3631\t3652.*$"/>
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176 <has_line_matching expression="^.*22\t1\t22\ttcaccgggagaaaaactggtgt\tchrII:11534525-11540624\t22\t3382\t3403.*$"/>
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177 <has_line_matching expression="^.*25\t1\t25\ttcaccgggtggaaactagcagtggc\tchrII:11534525-11540624\t25\t3060\t3084.*$"/>
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178 </assert_contents>
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179 </output>
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180 </test>
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181 </tests>
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182 <help>
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183 <![CDATA[
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184 **What MiRDeep2 Mapper does**
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185
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186 The mapper module is designed as a tool to process deep sequencing reads and/or map them to the reference genome.
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187 The module works in sequence space, and can process or map data that is in sequence fasta format.
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188 A number of the functions of the mapper module are implemented specifically with Solexa/Illumina data in mind.
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189
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190 **Example**
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191
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192 Processing reads and mapping them to a genome.
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193
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194 The -c option designates that the input file is a fasta file. The -j options removes entries with
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195 non-canonical letters (letters other than a,c,g,t,u,n,A,C,G,T,U,N). The -k option clips adapters. The -l option discards reads shorter than 18 nts.
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196 The -m option collapses the reads. The -p option maps the processed reads against the previously indexed genome (cel_cluster). The -s option
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197 designates the name of the output file of processed reads and the -t option designates the name of the output file of the genome mappings. Last,
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198 -v gives verbose output to the screen.
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199
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200 ``mapper.pl reads.fa -c -j -k TCGTATGCCGTCTTCTGCTTGT -l 18 -m -p cel_cluster -s reads_collapsed.fa -t reads_collapsed_vs_genome.arf -v``
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201
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202 ]]>
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203 </help>
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204 <citations>
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205 <citation type="doi">10.1093/nar/gkr688</citation>
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206 <citation type="doi">10.1002/0471250953.bi1210s36</citation>
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207 </citations>
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208 </tool>